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β-1,3-Glucanase from Delftia tsuruhatensis Strain MV01 and Its Potential Application in Vinification
被引:43
作者:
Blaettel, V.
[1
]
Larisika, M.
[1
]
Pfeiffer, P.
[1
]
Nowak, C.
[3
]
Eich, A.
[2
]
Eckelt, J.
[2
]
Koenig, H.
[1
]
机构:
[1] Inst Microbiol & Wine Res, D-55128 Mainz, Germany
[2] WEE Solve GmbH, D-55130 Mainz, Germany
[3] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
关键词:
LACTIC-ACID BACTERIA;
WINE SPOILAGE YEASTS;
CELL-WALL;
EXOPOLYSACCHARIDE PRODUCTION;
SACCHAROMYCES-CEREVISIAE;
PEDIOCOCCUS-PARVULUS;
HANSENIASPORA-UVARUM;
OENOCOCCUS-OENI;
GENE;
PURIFICATION;
D O I:
10.1128/AEM.01943-10
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
During vinification microbial activities can spoil wine quality. As the wine-related lactic acid bacterium Pediococcus parvulus is able to produce slimes consisting of a beta-1,3-glucan, must and wine filtration can be difficult or impossible. In addition, the metabolic activities of several wild-type yeasts can also negatively affect wine quality. Therefore, there is a need for measures to degrade the exopolysaccharide from Pediococcus parvulus and to inhibit the growth of certain yeasts. We examined an extracellular beta-1,3-glucanase from Delftia tsuruhatensis strain MV01 with regard to its ability to hydrolyze both polymers, the beta-1,3-glucan from Pediococcus and that from yeast cell walls. The 29-kDa glycolytic enzyme was purified to homogeneity. It exhibited an optimal activity at 50 degrees C and pH 4.0. The sequencing of the N terminus revealed significant similarities to beta-1,3-glucanases from different bacteria. In addition, the investigations indicated that this hydrolytic enzyme is still active under wine-relevant parameters such as elevated ethanol, sulfite, and phenol concentrations as well as at low pH values. Therefore, the characterized enzyme seems to be a useful tool to prevent slime production and undesirable yeast growth during vinification.
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页码:983 / 990
页数:8
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